4.8 Article

Mitochondrial DNA deletions are associated with non-B DNA conformations

Related references

Note: Only part of the references are listed.
Article Biochemistry & Molecular Biology

Human mitochondrial transcription factor A induces a U-turn structure in the light strand promoter

Anna Rubio-Cosials et al.

NATURE STRUCTURAL & MOLECULAR BIOLOGY (2011)

Article Biochemistry & Molecular Biology

The mitochondrial transcription and packaging factor Tfam imposes a U-turn on mitochondrial DNA

Huu B. Ngo et al.

NATURE STRUCTURAL & MOLECULAR BIOLOGY (2011)

Review Biochemistry & Molecular Biology

Somatic Mitochondrial DNA Mutations in Mammalian Aging

Nils-Goeran Larsson

ANNUAL REVIEW OF BIOCHEMISTRY, VOL 79 (2010)

Article Biochemistry & Molecular Biology

Helix Unwinding and Base Flipping Enable Human MTERF1 to Terminate Mitochondrial Transcription

Elena Yakubovskaya et al.

Review Biochemistry & Molecular Biology

Non-B DNA structure-induced genetic instability and evolution

Junhua Zhao et al.

CELLULAR AND MOLECULAR LIFE SCIENCES (2010)

Article Biochemistry & Molecular Biology

Mitochondrial RNA Polymerase Is Needed for Activation of the Origin of Light-Strand DNA Replication

Javier Miralles Fuste et al.

MOLECULAR CELL (2010)

Article Biochemistry & Molecular Biology

E. coli SbcCD and RecA Control Chromosomal Rearrangement Induced by an Interrupted Palindrome

Elise Darmon et al.

MOLECULAR CELL (2010)

Article Multidisciplinary Sciences

Origins and functional impact of copy number variation in the human genome

Donald F. Conrad et al.

NATURE (2010)

Review Genetics & Heredity

Triggers for genomic rearrangements: insights into genomic, cellular and environmental influences

Ram-Shankar Mani et al.

NATURE REVIEWS GENETICS (2010)

Article Biochemistry & Molecular Biology

Differential regulation of full-length genome and a single-stranded 7S DNA along the cell cycle in human mitochondria

Anita Antes et al.

NUCLEIC ACIDS RESEARCH (2010)

Article Genetics & Heredity

Repeats, longevity and the sources of mtDNA deletions: evidence from 'deletional spectra'

Xinhong Guo et al.

TRENDS IN GENETICS (2010)

Review Biochemistry & Molecular Biology

The inheritance of pathogenic mitochondrial DNA mutations

L. M. Cree et al.

BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE (2009)

Article Biochemistry & Molecular Biology

Circos: An information aesthetic for comparative genomics

Martin Krzywinski et al.

GENOME RESEARCH (2009)

Article Biochemistry & Molecular Biology

Native R-loops Persist throughout the Mouse Mitochondrial DNA Genome

Timothy A. Brown et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2008)

Article Biochemistry & Molecular Biology

Evidence for Variable Selective Pressures at a Large Secondary Structure of the Human Mitochondrial DNA Control Region

Filipe Pereira et al.

MOLECULAR BIOLOGY AND EVOLUTION (2008)

Article Genetics & Heredity

What causes mitochondrial DNA deletions in human cells?

Kim J. Krishnan et al.

NATURE GENETICS (2008)

Review Genetics & Heredity

Purifying selection of mtDNA and its implications for understanding evolution and mitochondrial disease

James Bruce Stewart et al.

NATURE REVIEWS GENETICS (2008)

Article Biotechnology & Applied Microbiology

PyCogent: a toolkit for making sense from sequence

Rob Knight et al.

GENOME BIOLOGY (2007)

Review Biochemistry & Molecular Biology

Non-B DNA conformations, mutagenesis and disease

Robert D. Wells

TRENDS IN BIOCHEMICAL SCIENCES (2007)

Article Multidisciplinary Sciences

Z-DNA-forming sequences generate large-scale deletions in mammalian cells

GL Wang et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2006)

Review Biochemistry & Molecular Biology

Post-transcriptional nucleotide modification and alternative folding of RNA

M Helm

NUCLEIC ACIDS RESEARCH (2006)

Article Multidisciplinary Sciences

Mutant mitochondrial helicase Twinkle causes multiple mtDNA deletions and a late-onset mitochondrial disease in mice

H Tyynismaa et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2005)

Review Genetics & Heredity

Mitochondrial DNA mutations in human disease

RW Taylor et al.

NATURE REVIEWS GENETICS (2005)

Article Biochemistry & Molecular Biology

Double-strand breaks of mouse muscle mtDNA promote large deletions similar to multiple mtDNA deletions in humans

S Srivastava et al.

HUMAN MOLECULAR GENETICS (2005)

Review Biochemistry & Molecular Biology

Advances in mechanisms of genetic instability related to hereditary neurological diseases

RD Wells et al.

NUCLEIC ACIDS RESEARCH (2005)

Article Biochemistry & Molecular Biology

MUSCLE: multiple sequence alignment with high accuracy and high throughput

RC Edgar

NUCLEIC ACIDS RESEARCH (2004)

Article Multidisciplinary Sciences

Breakpoints of gross deletions coincide with non-B DNA conformations

A Bacolla et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2004)

Article Genetics & Heredity

Two direct repeats cause most human mtDNA deletions

DC Samuels et al.

TRENDS IN GENETICS (2004)

Article Biochemistry & Molecular Biology

Twinkle and POLG defects enhance age-dependent accumulation of mutations in the control region of mtDNA

S Wanrooij et al.

NUCLEIC ACIDS RESEARCH (2004)

Article Multidisciplinary Sciences

Premature ageing in mice expressing defective mitochondrial DNA polymerase

A Trifunovic et al.

NATURE (2004)

Review Genetics & Heredity

Mitochondrial genomes: anything goes

G Burger et al.

TRENDS IN GENETICS (2003)

Article Biochemistry & Molecular Biology

Mitochondrial DNA replication: What we know

DA Clayton

IUBMB LIFE (2003)

Article Multidisciplinary Sciences

Topological challenges to DNA replication: Conformations at the fork

L Postow et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2001)

Article Biochemistry & Molecular Biology

Replication slippage involves DNA polymerase pausing and dissociation

E Viguera et al.

EMBO JOURNAL (2001)

Article Biochemistry & Molecular Biology

Human mtDNA sublimons resemble rearranged mitochondrial genoms found in pathological states

OA Kajander et al.

HUMAN MOLECULAR GENETICS (2000)